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BioWorld - Thursday, February 19, 2026
Home » Topics » Regulatory » EMA

EMA
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Roche reports on third quarter of 2010

Nov. 18, 2010

EMA approves Cell Therapeutics' pediatric investigation plan for Pixuvri

Nov. 17, 2010

EMA orphan drug status for SBC-102 in LAL deficiency / News in Context

Nov. 17, 2010

EMA committee recommends orphan drug status for ThermoDox in primary liver cancer

Nov. 12, 2010

Schering-Plough Europe withdraws MAA for Zenhale

Nov. 11, 2010

MabThera approved in E.U. as maintenance treatment of follicular lymphoma

Nov. 4, 2010

Genta receives EMA advice for phase III tesetaxel trial in gastric cancer

Nov. 3, 2010

E.U. grants authorization for Ruconest in hereditary angioedema

Oct. 29, 2010

EMA recommends changes in prescribing information for Invirase

Oct. 26, 2010

CHMP recommends new indication for Bristol-Myers Squibb's Sprycel

Oct. 26, 2010
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